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Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
- 2026-06-24FDA-DrugIntegraDose Compounding Services LLCClass IIIntegraDose Vasopressin syringes recalled for subpotency
IntegraDose Compounding Services LLC is recalling Vasopressin 2 Units/2 mL syringes because the drug may contain less active ingredient than labeled. This affects two specific lots distributed nationwide. No injuries have been reported.
- 2026-06-24FDA-DrugPAI Holdings LLCClass IIVistaPharm Kerr Insta-Char recalled for failing OTC standards
VistaPharm's Kerr Insta-Char activated charcoal product did not meet the required Over-the-Counter (OTC) Monograph standards set by the FDA. The affected product is a 240 mL bottle containing 50 grams of activated charcoal in a sorbitol base with cherry flavor (Lot #AH001, expiring 8/31/2026).
- 2026-06-24FDA-DrugPAI Holdings LLCClass IIVistaPharm Kerr Insta-Char recalled for OTC compliance failure
VistaPharm's Kerr Insta-Char activated charcoal suspension did not meet the standards required for over-the-counter products. The product was distributed nationwide, and affected lots should not be used.
- 2026-06-24FDA-DrugPAI Holdings LLCClass IIVistaPharm Kerr Insta-Char recalled for quality standards failure
VistaPharm's Kerr Insta-Char activated charcoal product did not meet the required OTC Monograph M023 standards set by the FDA. The affected product is a 240 ml bottle containing 50 grams of activated charcoal with cherry flavor (Lot #AE001, expiring 5/31/2026) distributed nationwide.
- 2026-06-24FDA-DrugPAI Holdings LLCClass IIVistaPharm Kerr Insta-Char recalled for not meeting OTC standards
VistaPharm's Kerr Insta-Char activated charcoal product failed to meet required Over-the-Counter (OTC) monograph standards. The product may not perform as intended or meet quality requirements for safety and effectiveness.
- 2026-06-24FDA-DrugGlenmark Pharmaceuticals Inc., USAClass IIGlenmark Alyacen 7/7/7 birth control recalled for impurity levels
Glenmark Pharmaceuticals is recalling specific lots of Alyacen 7/7/7 (a birth control pill) because testing found higher-than-allowed impurity levels in the tablets. The affected lots were distributed nationwide. No injuries have been reported.
- 2026-06-23NHTSA-EquipmentRockford CorporationRockford Fosgate amplifier kits recalled for fire risk
Certain Rockford Fosgate amplifier models (20GLADR-STG5, 24WRNGLR-FOX, 24WRNGLER-STG3, and 18WRNGLER-STG5) contain a 150-amp fuse that may not protect the circuit properly if a short circuit occurs. This inadequate protection could increase the risk of fire.
- 2026-06-19NHTSA-EquipmentAirxcel, Inc.Airxcel MaxxAir rooftop fan recalled for fire risk
Certain Airxcel MaxxAir N-Series Maxxfan rooftop ventilation fans have a printed circuit board that may overheat during operation. An overheated board increases the risk of fire.
- 2026-06-18FDA-PRMorningstar FarmsMorningStar Farms plant-based nuggets and sausage recalled for plastic
MorningStar Farms is recalling two products because they may contain plastic pieces. The affected items are Buffalo Chik'n Nuggets (10.5 oz) and Hot & Spicy Sausage Patties (8 oz) with specific "Better if Used Before" dates in early July 2027.
- 2026-06-18CPSCCooCooBaby, of ChinaCooCooBaby baby loungers recalled for suffocation risk
CooCooBaby Classic and Deluxe Baby Loungers have design flaws that create unsafe sleeping conditions for infants. The sides are too short to keep a baby secure, the sleeping pad is too thick and can cause suffocation, and babies can fall out or get trapped at the foot opening.
- 2026-06-18CPSCJoolz USA Inc., of New York, New YorkJoolz Aer2 Car Seat Adapters recalled for fall hazard
Joolz Aer2 Car Seat Adapters can fail to attach properly to Joolz Aer2 strollers, allowing the car seat to fall. The company has received one report of the adapters detaching. No injuries have been reported so far.
- 2026-06-18CPSCSHEIN Distribution Corporation, of Los Angeles, CaliforniaMichley children's pajamas recalled for burn hazard
SHEIN Distribution Corporation is recalling Michley-branded children's pajamas sold online because they don't meet mandatory flammability standards for sleepwear. The recalled one-piece pajamas came in green, pink, yellow, and purple with animal patches, in sizes 80–130. They pose a risk of serious burn injuries.
- 2026-06-18CPSCBada Boom Fireworks, of Blakeslee, PennsylvaniaBada Boom Pyro Diablo fireworks recalled for explosion risk
Bada Boom Fireworks is recalling Pyro Diablo "Diablo Rising" 9-shot fireworks (model PD-C5001) sold at their Pennsylvania locations. The fireworks contain too much explosive material and violate federal safety limits for aerial devices, creating a serious risk of unexpected explosions and severe burns.
- 2026-06-18CPSC7111495 Canada Inc., dba Arizer Tech, of Waterloo, OntarioArizer Solo III vaporizers recalled for fire risk
Arizer Solo III portable vaporizers with certain serial numbers contain a defective lithium-ion battery that can overheat, explode, or ignite, posing a serious fire and burn risk. The company has received four reports of batteries exploding or catching fire. About 5,000 units sold between May 2025 and January 2026 are affected.
- 2026-06-18CPSCShenzhen City ShengRu Fu Shi Company Ltd., doing business as Veseacky, of ChinaVeseacky pajama sets recalled for burn hazard
Veseacky children's pajama sets sold on Amazon do not meet mandatory federal safety standards for sleepwear and pose a risk of serious burns to children. The sets consist of a long-sleeve button-up top and matching pants, sold in various colors and prints from October 2020 through January 2026.
- 2026-06-18CPSCShenzhen Fuxiangyue Technology Co., Ltd., dba Arrogantf, of ChinaArrogantf spa drain covers recalled for entrapment hazard
Arrogantf white spa and hot tub drain covers do not meet federal safety standards for entrapment protection. They pose a risk of serious injury or death from entrapment and drowning, particularly to children. About 340 units were sold online through Amazon between September 2025 and March 2026.
- 2026-06-18CPSCGOPO Toys LLC, of San Bernardino, CaliforniaGOPO Toys teething toy recalled for choking risk
GOPO Toys pull string teething toys have silicone strings that are longer and thinner than safety standards allow. The strings can reach the back of a child's throat and become lodged, causing choking or respiratory distress. The company has received three reports of strings reaching children's throats.
- 2026-06-18CPSCHuizhou Huitong Crafts Co. Ltd., of ChinaBABESIDE doll stroller set recalled for choking hazard
BABESIDE toy sets sold on Amazon contain small parts that pose a choking risk to children under 3: a pacifier and a plush bear with detachable eyes. These pieces are not safe for young children and violate federal small parts rules.
- 2026-06-18USDAClass IIPower Plate Meals meatloaf recalled for undeclared soy
Power Plate Meals frozen meatloaf with garlic mashed potatoes contains soy, a known allergen, that is not listed on the package label. The affected products were produced between June 25, 2025, and June 10, 2026, and were sold in Minnesota, North Dakota, and South Dakota. No injuries have been reported.
- 2026-06-17FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific Orca valve recalled for suction button sticking
Boston Scientific is removing Orca Sterile Single Use Air/Water and Suction Valves from distribution because the suction button is sticking more often than expected. These valves are used during gastrointestinal endoscopic procedures to control air and water flow on endoscopes. No injuries have been reported.
- 2026-06-17FDA-DeviceAVID Medical, Inc.Class IIHalyard Eye Bag Pack recalled for sterilization failure
AVID Medical, Inc. distributed 60 kits of Halyard Eye Bag Pack (Kit Code UIEB48-01) with sealed pouches that did not undergo validated sterilization. The affected kits were distributed nationwide in Iowa. No injuries have been reported.
- 2026-06-17FDA-DeviceAVID Medical, Inc.Class IIHalyard Drape Pack recalled for unsterilized pouches
Halyard Drape Pack kits (Code LMDP36-01) were distributed without proper sterilization validation. Approximately 72 kits shipped with sealed pouches that had not undergone the required sterilization process. These kits were distributed nationwide and in Iowa.
- 2026-06-17FDA-DeviceAVID Medical, Inc.Class IIHalyard Towel Six Pack recalled for sterilization failure
AVID Medical inadvertently distributed 224 kits of Halyard Towel Six Pack (Kit Code AMTS70-01) with sealed pouches that had not undergone validated sterilization. The affected kits were distributed nationwide, with concentration in Iowa. No injuries have been reported.
- 2026-06-17FDA-DeviceAVID Medical, Inc.Class IIHalyard Pain Pack Kit recalled for unsterilized pouches
AVID Medical distributed 120 sealed Halyard Pain Pack kits (Kit Code AMPK48-01, Lot 334669) that did not undergo proper sterilization validation. The affected kits were distributed nationwide, with known distribution in Iowa. No injuries have been reported.
- 2026-06-17FDA-DeviceElekta, Inc.Class IIElekta MOSAIQ cancer treatment software may fail to load plans
Elekta's MOSAIQ Oncology Information System software (version 3.2) may fail to load an adapted baseline shift plan during cancer treatment delivery if a communication error occurs. This could affect the accuracy of radiation therapy positioning. No injuries have been reported.
- 2026-06-17FDA-DeviceAbbott MedicalClass IIAbbott Merlin PCS 3650 programmer software recalled for test termination malfunction
Abbott's Merlin PCS 3650 programmer software (versions 25.0.1 through 28.7.1) may malfunction during pacing capture threshold tests on pacemakers. When this occurs, the programmer may fail to successfully send the command to stop the test.
- 2026-06-17FDA-DeviceBoston Scientific Neuromodulation CorporationClass IIBoston Scientific Clik X Anchor recalled for sterility concerns
Boston Scientific is recalling the Model SC-4318 Clik X Anchor (Lot #35107836) because sterile anchors may lack proper sterility assurance. Approximately 43 units were distributed across six U.S. states.
- 2026-06-17FDA-DeviceBoston Scientific Neuromodulation CorporationClass IIBoston Scientific TCN Electrodes recalled for performance issues
Boston Scientific has recalled certain reusable TCN Electrodes used in neuromodulation devices because they may not perform as expected. The affected electrodes come in multiple sizes and configurations, with about 49,251 units distributed worldwide.
- 2026-06-17FDA-DeviceBoston Scientific Neuromodulation CorporationClass IIBoston Scientific CSK Electrodes recalled for performance issues
Boston Scientific has recalled certain CSK Electrode models used in neuromodulation procedures because they may not perform reliably as intended. The affected electrodes come in multiple configurations and lengths. No injuries have been reported to date.
- 2026-06-17FDA-DeviceFresenius Medical Care Holdings, Inc.Class IIFresenius Bicarby Dialysate recalled for GTIN labeling error
Fresenius Medical Care's Bicarby Dialysate (Model RFP-400-G) has incorrect barcode labeling on some units. While the case label and printed information are correct, scanning the GTIN barcode alone could lead to identification errors. This could result in use of a dialysate with a potassium concentration different from what was prescribed.